FI79547C - Kväve och fosfor innehållande funktionella vätskor och vattenhaltiga s ystem innehållande dessa - Google Patents
Kväve och fosfor innehållande funktionella vätskor och vattenhaltiga s ystem innehållande dessa Download PDFInfo
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- FI79547C FI79547C FI853835A FI853835A FI79547C FI 79547 C FI79547 C FI 79547C FI 853835 A FI853835 A FI 853835A FI 853835 A FI853835 A FI 853835A FI 79547 C FI79547 C FI 79547C
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- component
- carbon atoms
- acid
- aqueous
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- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title claims description 27
- 239000000203 mixture Substances 0.000 claims description 89
- 229920000768 polyamine Polymers 0.000 claims description 60
- 150000001412 amines Chemical class 0.000 claims description 52
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 46
- 239000003795 chemical substances by application Substances 0.000 claims description 43
- 239000012530 fluid Substances 0.000 claims description 37
- 125000004432 carbon atom Chemical group C* 0.000 claims description 36
- 239000002253 acid Substances 0.000 claims description 33
- 239000012141 concentrate Substances 0.000 claims description 26
- 229910052698 phosphorus Inorganic materials 0.000 claims description 26
- 239000011574 phosphorus Substances 0.000 claims description 26
- 229910052717 sulfur Chemical group 0.000 claims description 20
- 125000002947 alkylene group Chemical group 0.000 claims description 18
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 17
- 239000000654 additive Substances 0.000 claims description 17
- 239000011593 sulfur Chemical group 0.000 claims description 17
- 125000003118 aryl group Chemical group 0.000 claims description 15
- 239000007788 liquid Substances 0.000 claims description 15
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 14
- 125000001931 aliphatic group Chemical group 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 150000002430 hydrocarbons Chemical group 0.000 claims description 12
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- 239000000314 lubricant Substances 0.000 claims description 10
- 229920000098 polyolefin Polymers 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
- 239000005977 Ethylene Substances 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
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- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 6
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 claims description 6
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 5
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- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 claims description 5
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- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 5
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 150000008064 anhydrides Chemical class 0.000 claims description 3
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- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- 229920002367 Polyisobutene Polymers 0.000 claims description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 claims description 2
- NHWGPUVJQFTOQX-UHFFFAOYSA-N ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium Chemical compound CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC NHWGPUVJQFTOQX-UHFFFAOYSA-N 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 62
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- 241001465754 Metazoa Species 0.000 description 17
- 125000001424 substituent group Chemical group 0.000 description 15
- 125000000623 heterocyclic group Chemical group 0.000 description 14
- 238000000034 method Methods 0.000 description 14
- 150000001336 alkenes Chemical class 0.000 description 11
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 10
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- 229940014800 succinic anhydride Drugs 0.000 description 9
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 8
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- 239000002184 metal Substances 0.000 description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 8
- 241000283973 Oryctolagus cuniculus Species 0.000 description 7
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- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 241000700159 Rattus Species 0.000 description 6
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- 229910019142 PO4 Inorganic materials 0.000 description 5
- 230000000844 anti-bacterial effect Effects 0.000 description 5
- 239000003899 bactericide agent Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
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- 238000002156 mixing Methods 0.000 description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000000376 reactant Substances 0.000 description 5
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 230000010933 acylation Effects 0.000 description 4
- 238000005917 acylation reaction Methods 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
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- 235000011007 phosphoric acid Nutrition 0.000 description 4
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- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 3
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
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- 125000001302 tertiary amino group Chemical group 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 2
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
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- DMEGYFMYUHOHGS-UHFFFAOYSA-N cycloheptane Chemical group C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 2
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- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
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- YISRDGYZLHFSJW-UHFFFAOYSA-N (2-pentylphenyl) dihydrogen phosphite Chemical compound CCCCCC1=CC=CC=C1OP(O)O YISRDGYZLHFSJW-UHFFFAOYSA-N 0.000 description 1
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- DIIIISSCIXVANO-UHFFFAOYSA-N 1,2-Dimethylhydrazine Chemical compound CNNC DIIIISSCIXVANO-UHFFFAOYSA-N 0.000 description 1
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- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 1
- WTGGXKMCUUXBQR-UHFFFAOYSA-N 1-butyl-2-(4-methylphenyl)hydrazine Chemical compound CCCCNNC1=CC=C(C)C=C1 WTGGXKMCUUXBQR-UHFFFAOYSA-N 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
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- IIEJSCPJXISDFF-UHFFFAOYSA-N 1-methyl-2-(4-nitrophenyl)hydrazine Chemical compound CNNC1=CC=C([N+]([O-])=O)C=C1 IIEJSCPJXISDFF-UHFFFAOYSA-N 0.000 description 1
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
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- 150000003235 pyrrolidines Chemical class 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 231100000161 signs of toxicity Toxicity 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- NMWCVZCSJHJYFW-UHFFFAOYSA-M sodium;3,5-dichloro-2-hydroxybenzenesulfonate Chemical compound [Na+].OC1=C(Cl)C=C(Cl)C=C1S([O-])(=O)=O NMWCVZCSJHJYFW-UHFFFAOYSA-M 0.000 description 1
- 230000000392 somatic effect Effects 0.000 description 1
- 238000012453 sprague-dawley rat model Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 210000000434 stratum corneum Anatomy 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- DIORMHZUUKOISG-UHFFFAOYSA-N sulfoformic acid Chemical class OC(=O)S(O)(=O)=O DIORMHZUUKOISG-UHFFFAOYSA-N 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000004853 tetrahydropyridinyl group Chemical group N1(CCCC=C1)* 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- NEUOBESLMIKJSB-UHFFFAOYSA-J tetrasodium;tetraacetate Chemical compound [Na+].[Na+].[Na+].[Na+].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O NEUOBESLMIKJSB-UHFFFAOYSA-J 0.000 description 1
- 125000004149 thio group Chemical group *S* 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 150000004886 thiomorpholines Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- QQBLOZGVRHAYGT-UHFFFAOYSA-N tris-decyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OCCCCCCCCCC QQBLOZGVRHAYGT-UHFFFAOYSA-N 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- NIMODYJOEUHTAF-UHFFFAOYSA-L zinc;dicyclohexyloxy-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].C1CCCCC1OP(=S)([S-])OC1CCCCC1.C1CCCCC1OP(=S)([S-])OC1CCCCC1 NIMODYJOEUHTAF-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/123—Reaction products obtained by phosphorus or phosphorus-containing compounds, e.g. P x S x with organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/043—Ammonium or amine salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/047—Thioderivatives not containing metallic elements
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/061—Metal salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/065—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/01—Emulsions, colloids, or micelles
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Claims (25)
1. Vattenbaserad komposition, som är användbar som funktiona11 vätska, sAsom smörjmedel, hydraulolja eller 5 skärolja, kännetecknad därav, att den innehAl-ler som tillsatsämne en i vatten dispergerad reaktionspro-dukt, som bildats av A) Atminstone ett karboxylsyra-acyleringsämne med formeln
2. Komposition enligt patentkravet 1, kännetecknad därav, att komponenternas A) och C) förhAl-lande till komponent B) är Atminstone en halv ekvivalent av komponenter A) och C) per en mol av komponent B).
3. Komposition enligt patentkravet 1, känne tecknad därav, att komponent B) innehAller 5 HN<-grupper per en mol, och ungefär 0,5 - 4,5 ekvivalenter av vardera komponenten A) och C) har omsatts med komponenten B).
4. Komposition enligt patentkravet 1, k ä n n e - 53 7 9 5 4 7 t e c k n a d därav, att 1 komponent A) är kolvätesubs-tituenten R en C1 - ungefär Cx 0-kolvätegrupp.
5. Komposition enligt patentkravet 1, känne-t e c k n a d därav, att i komponent A) innehäller kol- 5 vätesubstituenten R i medeltal minst ungefär 12 kolatomer.
6. Komposition enligt patentkravet 5, känne-t e c k n a d därav, att koivätesubstituenten innehäller minst ungefär 18 kolatomer.
7. Komposition enligt patentkravet 5, känne-10 tecknad därav, att kolvätesubstituenten har här- letts ur polyisobuten.
8. Komposition enligt patentkravet 1, känne-tecknad därav, att komponent B) är en monoamin el-ler polyamin.
9. Komposition enligt patentkravet 1, känne- tecknad därav, att komponent B) är hydrazin eller en substituerad hydrazin.
10 R3 R4 där n är ett heltal mellan 1 och ungefär 10; vardera R3, R4 och R5 är självständigt en väteatom, kolvätegrupp eller hydroxisubstituerad kolvätegrupp med i medeltal ungefär 40 kolatomer, och alkylengruppen innehäller i medeltal 15 1 - ungefär 10 kolatomer.
10. Komposition enligt patentkravet 1, känne-tecknad därav, att komponent B) är en alifatisk, 20 cykloalifatisk eller aromatisk monoamin eller polyamin.
10 R-CHCOOH .0 I f CH-COOH eller R-CH-C l > CH;-\ 15 där R är en kolvätegrupp, B) Atminstone en amin som i strukturen innehAller Atminstone en HN>-grupp, ooh C) Atminstone en fosfor innehAilande syra med formeln
11. Komposition enligt patentkravet 1, känne-tecknad därav, att komponent B) är en monoamin med högst ungefär 40 kolatomer.
12. Komposition enligt patentkravet 1, känne-25 tecknad därav, att komponent B) är en hydroxiamin.
13. Komposition enligt patentkravet 1, känne-tecknad därav, att komponent B) är en aminosulfon-syra.
14. Komposition enligt patentkravet 1, känne-30 tecknad därav, att komponent B) är en kolvätepoly- amin, som framställts genom att omsätta en klorerad polyolefin med en molekylvikt av minst 400 med ammoniak eller en amin.
15. Komposition enligt patentkravet 1, känne-35 tecknad därav, att komponent B) är en förgrenad polyalkylenpolyamin. 54 79547
16. Komposition enligt patentkravet 1, k ä n nets c k n a d därav, att komponent B) är en polyoxialky-lendiamin eller polyoxialkylentriamin, varvid medelmole-kylvikten för denna diamin och triamin är minst ungefär 5 200.
17. Komposition enligt patentkravet 1, känne-t e c k n a d därav, att komponent B) är en alkylenpoly-amin med formeln H-N -(— alkylen-N·)^- R5
18. Komposition enligt patentkravet 17, känne-t e c k n a d därav, att vardera av grupperna R3, R4 och R5 innehäller självständigt i medeltal högst ungefär 30 kolatomer.
19. Komposition enligt patentkravet 17, känne- t e c k n a d därav, att alkylengruppen är etylen eller propyIen.
20. Komposition enligt patenktravet 1, känne-t e c k n a d därav, att komponent C) har formeln
25 R1 -O ^ S Il P-SH R2 -O
20 R' (X3 ) X2 —H P-X' H r2 (χ< )„, där vardera X', X2, X3 och X4 självständigt betecknar syre eller svavel, vardera m är 0 eller 1 och vardera R' och
25 R2 är självständigt en kolvätegrupp.
21. Komposition enligt patentkravet 1, känne-t e c k n a d därav, att komponent C) är di(alkyl)fosfor- 30 ditiosyra, där vardera alkylen innehäller självständigt ungefär 4 - ungefär 8 kolatomer.
22. Komposition enligt patentkravet 1, k ä n n e -t e c k n a d därav, att komponent C) är 0,0-di-(isook-tyl)fosforditiosyra.
23. Vattenbaserad komposition enligt patentkravet 1, som är användbar som funktionell vätska, känne-
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US58003384A | 1984-02-14 | 1984-02-14 | |
US58003384 | 1984-02-14 | ||
US8500159 | 1985-01-29 | ||
PCT/US1985/000159 WO1985003709A1 (en) | 1984-02-14 | 1985-01-29 | Nitrogen- and phosphorus-containing compositions and aqueous systems containing same |
Publications (4)
Publication Number | Publication Date |
---|---|
FI853835L FI853835L (fi) | 1985-10-03 |
FI853835A0 FI853835A0 (fi) | 1985-10-03 |
FI79547B FI79547B (fi) | 1989-09-29 |
FI79547C true FI79547C (sv) | 1990-01-10 |
Family
ID=24319381
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI853835A FI79547C (sv) | 1984-02-14 | 1985-10-03 | Kväve och fosfor innehållande funktionella vätskor och vattenhaltiga s ystem innehållande dessa |
Country Status (14)
Country | Link |
---|---|
US (2) | US4772739A (sv) |
EP (1) | EP0172225B1 (sv) |
JP (1) | JPH0826340B2 (sv) |
BR (1) | BR8505671A (sv) |
CA (1) | CA1258267A (sv) |
DE (1) | DE3572492D1 (sv) |
ES (1) | ES8606366A1 (sv) |
FI (1) | FI79547C (sv) |
IN (1) | IN163405B (sv) |
IT (1) | IT1182198B (sv) |
MX (1) | MX166753B (sv) |
NO (1) | NO168179C (sv) |
WO (1) | WO1985003709A1 (sv) |
ZA (1) | ZA85940B (sv) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3572492D1 (en) * | 1984-02-14 | 1989-09-28 | Lubrizol Corp | Nitrogen- and phosphorus-containing compositions and aqueous systems containing same |
US4618450A (en) * | 1984-11-07 | 1986-10-21 | The Lubrizol Corporation | Aqueous systems containing amino sulfonic acid derivatives of carboxylic acids |
US4770803A (en) * | 1986-07-03 | 1988-09-13 | The Lubrizol Corporation | Aqueous compositions containing carboxylic salts |
US5527491A (en) | 1986-11-14 | 1996-06-18 | The Lubrizol Corporation | Emulsifiers and explosive emulsions containing same |
US4919178A (en) * | 1986-11-14 | 1990-04-24 | The Lubrizol Corporation | Explosive emulsion |
US5129972A (en) | 1987-12-23 | 1992-07-14 | The Lubrizol Corporation | Emulsifiers and explosive emulsions containing same |
US5080813A (en) * | 1990-03-26 | 1992-01-14 | Ferro Corporation | Lubricant composition containing dialkyldithiophosphoric acid neutralized with alkoxylated aliphatic amines |
DE69033375T2 (de) * | 1990-04-02 | 2000-05-11 | Ethyl Petroleum Additives Ltd., Bracknell | Schmiermittelzusammensetzungen und Additive dafür |
US5260051A (en) * | 1990-12-17 | 1993-11-09 | Lever Brothers Company, Division Of Conopco, Inc. | Compositions comprising phosphate ester compounds containing a beneficial reagent component |
US5328619A (en) * | 1991-06-21 | 1994-07-12 | Ethyl Petroleum Additives, Inc. | Oil additive concentrates and lubricants of enhanced performance capabilities |
EP0712434B1 (en) * | 1993-08-03 | 2000-03-22 | Infineum USA L.P. | Low molecular weight basic nitrogen-containing reaction products as enhanced phosphorus/boron carriers in lubrication oils |
FR2710918B1 (fr) * | 1993-10-06 | 1995-12-01 | Inst Francais Du Petrole | Compositions lubrifiantes contenant un phosphate d'amine comportant un cycle imide terminal. |
US5520831A (en) * | 1993-12-20 | 1996-05-28 | Exxon Chemical Patents Inc. | Increasing the friction durability of power transmission fluids through the use of oil soluble competing additives |
DE69432153T2 (de) * | 1993-12-20 | 2003-11-27 | Infineum Usa L.P., Linden | Erhöhung der reibungsbeständigkeit von kraftübertragungsflüssigkeiten durch die verwendung von öllöslichen konkurierenden additiven |
KR100240364B1 (ko) * | 1993-12-20 | 2000-01-15 | 만셀 케이쓰 로드니 | 유성 조성물의 정류 마찰계수를 증가시키는 방법 |
Family Cites Families (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2737492A (en) * | 1952-03-26 | 1956-03-06 | American Cyanamid Co | Lubricating oil compositions |
US3103492A (en) * | 1958-07-30 | 1963-09-10 | Lubricating composition | |
US3058910A (en) * | 1958-10-24 | 1962-10-16 | Hall Stewart | Oil additive concentrate |
US3074990A (en) * | 1958-12-29 | 1963-01-22 | Universal Oil Prod Co | Alkylthiophosphoric acid salt of polymeric condensation product and use thereof |
GB1009197A (en) * | 1961-08-30 | 1965-11-10 | Lubrizol Corp | Stable water-in-oil emulsion |
US3197405A (en) * | 1962-07-09 | 1965-07-27 | Lubrizol Corp | Phosphorus-and nitrogen-containing compositions and process for preparing the same |
US3133787A (en) * | 1962-09-04 | 1964-05-19 | Socony Mobil Oil Co Inc | Corrosion inhibition |
US3185645A (en) * | 1962-09-28 | 1965-05-25 | California Research Corp | Oxidation inhibited lubricants |
US3184412A (en) * | 1962-09-28 | 1965-05-18 | California Research Corp | Lubricants inhibited against oxidation |
US3201447A (en) * | 1962-11-29 | 1965-08-17 | Universal Oil Prod Co | Ether amine salts of dithiophosphoric acid mono and diesters |
GB1044810A (en) * | 1963-05-14 | 1966-10-05 | Lubrizol Corp | Organic phosphinodithioate-amine reaction products |
GB1054093A (sv) * | 1963-06-17 | |||
GB1084036A (sv) * | 1963-12-12 | 1900-01-01 | ||
US3484504A (en) * | 1963-12-12 | 1969-12-16 | Universal Oil Prod Co | Addition reaction product of oxyalkylenated phosphorus compounds and n-containing polymers and use thereof |
US3359347A (en) * | 1963-12-12 | 1967-12-19 | Universal Oil Prod Co | Addition reaction products of oxyalkylenated phosphorus compounds and nu-containing polymers |
US3484374A (en) * | 1963-12-12 | 1969-12-16 | Universal Oil Prod Co | Stabilization or organic substances |
US3320164A (en) * | 1965-07-14 | 1967-05-16 | Brunel Henri | Non-corrosive, lubricating, cutting and cooling additives |
US3519563A (en) * | 1967-10-31 | 1970-07-07 | Chevron Res | Thiophosphate salts of aralkylene diamines as antiwear,extreme pressure and oxidation inhibitor agents |
DE1719543B2 (de) * | 1968-02-17 | 1976-06-16 | Verfahren zur antielektrostatischen ausruestung von faeden, fasern und textilien aus polyester oder polyamid | |
GB1357745A (en) * | 1971-05-05 | 1974-06-26 | Exxon Research Engineering Co | Lubricating oil compositions |
US3826745A (en) * | 1972-06-30 | 1974-07-30 | Exxon Research Engineering Co | Compositions containing metal dialkyl dithiophosphates are inhibited against haze and precipitates by amine salts of mixed acid phosphates |
US4085054A (en) * | 1973-10-18 | 1978-04-18 | Giancarlo Bussi | Utilization of orthophosphoric esters for the production of aqueous fluids for working metals |
US4160089A (en) * | 1973-10-18 | 1979-07-03 | Aquila S.P.A. | Utilization of orthophosphoric esters for the production of aqueous fluids for working metals |
CA1025878A (en) * | 1973-12-12 | 1978-02-07 | The Lubrizol Corporation | Phosphorus, nitrogen and sulfo-containing additives |
US3926821A (en) * | 1973-12-12 | 1975-12-16 | Lubrizol Corp | Phosphorus, nitrogen and sulfo-containing additives |
DE2608836C3 (de) * | 1976-03-04 | 1982-02-18 | Rhein-Chemie Rheinau Gmbh, 6800 Mannheim | Geschwefelte Phosphorsäure-ester-salze |
US4257902A (en) * | 1976-08-04 | 1981-03-24 | Singer & Hersch Industrial Development (Pty.) Ltd. | Water-based industrial fluids |
US4101427A (en) * | 1977-02-09 | 1978-07-18 | Exxon Research & Engineering Co. | Lubricant composition |
US4215002A (en) * | 1978-07-31 | 1980-07-29 | Texaco Inc. | Water-based phosphonate lubricants |
US4329249A (en) * | 1978-09-27 | 1982-05-11 | The Lubrizol Corporation | Carboxylic acid derivatives of alkanol tertiary monoamines and lubricants or functional fluids containing the same |
EP0014288B1 (en) * | 1978-12-07 | 1983-06-08 | Exxon Research And Engineering Company | Process for producing oil soluble derivatives of unsaturated c4-c10 dicarboxylic acid materials |
US4234435A (en) * | 1979-02-23 | 1980-11-18 | The Lubrizol Corporation | Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation |
US4368133A (en) * | 1979-04-02 | 1983-01-11 | The Lubrizol Corporation | Aqueous systems containing nitrogen-containing, phosphorous-free carboxylic solubilizer/surfactant additives |
US4253975A (en) * | 1979-08-27 | 1981-03-03 | Mobil Oil Corporation | Aqueous lubricants containing metal hydrocarbyl dithiophosphates |
JPS6050398B2 (ja) * | 1980-03-22 | 1985-11-08 | 本田技研工業株式会社 | 水溶性油剤 |
US4338205A (en) * | 1980-08-25 | 1982-07-06 | Exxon Research & Engineering Co. | Lubricating oil with improved diesel dispersancy |
US4721802A (en) * | 1983-01-07 | 1988-01-26 | The Lubrizol Corporation | Dithiophosphorus/amine salts |
DE3572492D1 (en) * | 1984-02-14 | 1989-09-28 | Lubrizol Corp | Nitrogen- and phosphorus-containing compositions and aqueous systems containing same |
-
1985
- 1985-01-29 DE DE8585901171T patent/DE3572492D1/de not_active Expired
- 1985-01-29 EP EP85901171A patent/EP0172225B1/en not_active Expired
- 1985-01-29 WO PCT/US1985/000159 patent/WO1985003709A1/en active IP Right Grant
- 1985-01-29 BR BR8505671A patent/BR8505671A/pt not_active IP Right Cessation
- 1985-01-29 JP JP60500812A patent/JPH0826340B2/ja not_active Expired - Lifetime
- 1985-02-07 ZA ZA85940A patent/ZA85940B/xx unknown
- 1985-02-08 CA CA000473870A patent/CA1258267A/en not_active Expired
- 1985-02-11 IN IN91/CAL/85A patent/IN163405B/en unknown
- 1985-02-13 ES ES540379A patent/ES8606366A1/es not_active Expired
- 1985-02-13 MX MX204319A patent/MX166753B/es unknown
- 1985-02-13 IT IT47681/85A patent/IT1182198B/it active
- 1985-10-03 FI FI853835A patent/FI79547C/sv not_active IP Right Cessation
- 1985-10-11 NO NO85854044A patent/NO168179C/no unknown
-
1986
- 1986-06-25 US US06/879,501 patent/US4772739A/en not_active Expired - Fee Related
-
1989
- 1989-09-07 US US07/405,074 patent/US5041598A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPS61501210A (ja) | 1986-06-19 |
US5041598A (en) | 1991-08-20 |
IT8547681A1 (it) | 1986-08-13 |
ZA85940B (en) | 1985-10-30 |
DE3572492D1 (en) | 1989-09-28 |
US4772739A (en) | 1988-09-20 |
FI79547B (fi) | 1989-09-29 |
MX166753B (es) | 1993-02-01 |
FI853835L (fi) | 1985-10-03 |
EP0172225B1 (en) | 1989-08-23 |
IN163405B (sv) | 1988-09-17 |
ES8606366A1 (es) | 1986-04-16 |
JPH0826340B2 (ja) | 1996-03-13 |
NO854044L (no) | 1985-10-11 |
IT1182198B (it) | 1987-09-30 |
NO168179B (no) | 1991-10-14 |
ES540379A0 (es) | 1986-04-16 |
NO168179C (no) | 1992-01-22 |
EP0172225A1 (en) | 1986-02-26 |
IT8547681A0 (it) | 1985-02-13 |
BR8505671A (pt) | 1986-02-18 |
WO1985003709A1 (en) | 1985-08-29 |
FI853835A0 (fi) | 1985-10-03 |
CA1258267A (en) | 1989-08-08 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM | Patent lapsed | ||
MM | Patent lapsed |
Owner name: THE LUBRIZOL CORPORATION |